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Catalog Number:
15235
CAS Number:
208404-16-4
Boc-(3-pyridyl)-L-β-homoalanine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-β-HomoAla(3-pyridyl)-OH, Boc-(S-3-amino-4-(3-pyridyl)butyric acid
Documents
$115.00 /25MG
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Product Information

Boc-(3-pyridyl)-L-b-homoalanine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers working in medicinal chemistry and biochemistry. Its unique pyridine ring structure contributes to its potential as a building block for bioactive peptides, allowing for the development of novel therapeutics with improved efficacy and selectivity.

In practical applications, Boc-(3-pyridyl)-L-b-homoalanine can be utilized in the synthesis of peptide-based drugs, particularly those targeting neurological disorders, due to its ability to mimic natural amino acids while providing enhanced properties. Its compatibility with various coupling reagents and methods further simplifies the peptide synthesis process, making it a valuable asset in pharmaceutical research and development. Researchers can leverage this compound to explore new avenues in drug design, ultimately contributing to advancements in healthcare.

Synonyms
Boc-L-β-HomoAla(3-pyridyl)-OH, Boc-(S-3-amino-4-(3-pyridyl)butyric acid
CAS Number
208404-16-4
Purity
≥ 99% (HPLC)
Molecular Formula
C14H20N2O4
Molecular Weight
280.32
MDL Number
MFCD01861056
PubChem ID
53397918
Melting Point
188-193 °C
Appearance
Yellowish solid
Optical Rotation
[a]D25 = -12 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-β-HomoAla(3-pyridyl)-OH, Boc-(S-3-amino-4-(3-pyridyl)butyric acid
CAS Number
208404-16-4
Purity
≥ 99% (HPLC)
Molecular Formula
C14H20N2O4
Molecular Weight
280.32
MDL Number
MFCD01861056
PubChem ID
53397918
Melting Point
188-193 °C
Appearance
Yellowish solid
Optical Rotation
[a]D25 = -12 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(3-pyridyl)-L-b-homoalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in creating modified peptides that can enhance biological activity.
  • Drug Development: It plays a role in the development of pharmaceuticals, especially in designing compounds that target specific receptors, which can lead to more effective treatments.
  • Bioconjugation: The chemical is used in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, improving their delivery and efficacy.
  • Research in Neuroscience: Its structural features make it useful in studying neuroactive compounds, potentially leading to breakthroughs in understanding neurological disorders.
  • Custom Synthesis: This compound is often employed in custom synthesis projects for academic and industrial research, providing flexibility in creating tailored compounds for specific applications.

Citations